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Sr. Clinical Research Associate

Career

Sr. Clinical Research Associate

Your Exciting Role

  • Responsible for project management throughout project phases including initiation, design, execution, and completion, ensuring compliance with regulatory requirements and Good Clinical Practice (GCP).
  • Creating SOP, WI, WO, FORM, and others related to the document management system, especially in the scope of R&D project management. 
  • Responsible for controlling and monitoring project objectives, including clinical trial timelines, site performance, and regulatory compliance. 
  • Co-manage the reimbursable invoices reconciliation process. 
  • Responsible for exploring creative solutions for common project budget and timeline problems to ensure effective and transparent monitoring while mitigating risks in clinical research.
  • Identify and resolve any issues related to protocol deviations, adverse events, or compliance risks at the site. 
  • Develop relationships with clients and vendors, identifying moments to leverage emerging opportunities. 
  • Prepare weekly and monthly performance reports for timeline and budgeting of R&D projects.

Ideally, You Would Have

  • Passionate in preserving Indonesia biodiversity through sustainable innovations.
  • Bachelor of Science in Biology, Pharmaceuticals, Chemistry, Chemical/Industrial Engineering or other related major.
  • Has experience in Project Management, Clinical Research, Laboratory and the molecular biology techniques are an added value.
  • Good computer skills, experience with Microsoft Office also laboratory system.
  • Having a good communication and interpersonal skills. 
  • Thorough & nimble, finished report within time scheduled. 
  • Able to work with team.

Sr. Clinical Research Associate

Research & Development

Full-Time

Jakarta

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